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United States · US · US:70069-402_93e51046-a2f5-47ab-8aa7-b0d8c9c119eb

Bimatoprost

Orange BookUNIISPLATC S01EE03

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerSomerset Therapeutics, LLC
CountryUS (United States)
ATC codeS01EE03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7006940201
    1 BOTTLE in 1 CARTON (70069-402-01) / 5 mL in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
QXS94885MZ
BIMATOPROST
RxCUI 283810
Orange Book
A207601
AT
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "QXS94885MZ",
    "rxcui": "283810",
    "inchikey": "AQOKCDNYWBIDND-FTOWTWDKSA-N",
    "display_name": "BIMATOPROST",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "OPHTHALMIC",
  "spl_meta": {
    "6a74ad65-dd76-45c1-9bbe-4218a9978b70": {
      "match": "brand_token",
      "title": "BIMATOPROST SOLUTION/ DROPS [FIRST NATION GROUP, LLC]",
      "spl_version": "1",
      "published_date": "2026-05-01"
    }
  },
  "productid": "70069-402_93e51046-a2f5-47ab-8aa7-b0d8c9c119eb",
  "productndc": "70069-402",
  "dosage_form": "SOLUTION/ DROPS",
  "orange_book": {
    "appl_no": "207601",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AT",
        "strength": "0.03%",
        "product_no": "001",
        "approval_date": "Jun 19, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BIMATOPROST",
  "proprietary_name": "Bimatoprost",
  "active_ingred_unit": "mg/mL",
  "application_number": "ANDA207601",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Bimatoprost",
  "start_marketing_date": "20190619",
  "active_numerator_strength": ".3"
}

Related drugs

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